Handbook of Clinical Nanomedicine : Law, Business, Regulation, Safety and Risk

Book information

Publisher
[s.n.]
Year
2015
ISBN
978-981-4669-23-8, 9814669237, 978-981-4669-21-4
Format
PDF
Filesize
46 MB (48446559 bytes)
Series
Pan Stanford series on nanomedicine 1
Pages
\1686
Time added
2016-05-22 07:20:00

Description

This unique handbook (60 chapters) examines the entire "product life cycle," from the creation of nanomedical products to their final market introduction. While focusing on critical issues relevant to nanoproduct development and translational activities, it tackles topics such as regulatory science, patent law, FDA law, ethics, personalized medicine, risk analysis, toxicology, nano-characterization and commercialization activities. A separate section provides fascinating perspectives and editorials from leading experts in this complex interdisciplinary field. Read more... Abstract: This unique handbook (60 chapters) examines the entire "product life cycle," from the creation of nanomedical products to their final market introduction. While focusing on critical issues relevant to nanoproduct development and translational activities, it tackles topics such as regulatory science, patent law, FDA law, ethics, personalized medicine, risk analysis, toxicology, nano-characterization and commercialization activities. A separate section provides fascinating perspectives and editorials from leading experts in this complex interdisciplinary field

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